FDA Grants Breakthrough Therapy Designation for Genentech’s Investigational Cancer Immunotherapy MPDL3280A (Anti-PDL1) in N...
02 Febrero 2015 - 12:00AM
Business Wire
-- Second FDA Breakthrough Therapy Designation
for MPDL3280A following bladder cancer in 2014 --
Genentech, a member of the Roche Group (SIX: RO, ROG; OTCQX:
RHHBY), announced today that it has received a second Breakthrough
Therapy Designation from the U.S. Food and Drug Administration
(FDA) for its investigational cancer immunotherapy MPDL3280A
(anti-PDL1). The designation was granted for the treatment of
people with PD-L1 (Programmed Death-Ligand 1) positive non-small
cell lung cancer (NSCLC) whose disease has progressed during or
after platinum-based chemotherapy (and an appropriate targeted
therapy for those with an EGFR mutation-positive or ALK-positive
tumor).
“Lung cancer is the leading cause of cancer death globally, and
we are pleased the FDA has granted breakthrough designation for
MPDL3280A in non-small cell lung cancer,” said Sandra Horning,
M.D., chief medical officer and head of Global Product Development.
“We are committed to personalized healthcare, developing medicines
like MPDL3280A with companion tests that may help us identify those
who may be appropriate candidates for our medicines.”
This Breakthrough Therapy Designation is based on early results
of MPDL3280A in people whose NSCLC was characterized as PD-L1
positive by an investigational test being developed by Roche. All
studies of MPDL3280A are prospectively evaluating PD-L1 expression.
Some studies will evaluate the medicine regardless of a tumor’s
PD-L1 status; other studies are evaluating the medicine only in
people whose tumors are characterized as PD-L1 positive.
Breakthrough Therapy Designation is designed to expedite the
development and review of medicines intended to treat serious
diseases and to help ensure patients have access to them through
FDA approval as soon as possible. The FDA granted the first
Breakthrough Therapy Designation for MPDL3280A in metastatic
bladder cancer in 2014. Ongoing pivotal studies of MPDL3280A
include lung and bladder cancer, and we plan to initiate Phase III
studies in additional tumor types this year.
About MPDL3280A (anti-PDL1)
MPDL3280A (also known as anti-PDL1 and RG7446) is an
investigational monoclonal antibody designed to interfere with a
protein called PD-L1. MPDL3280A is designed to target PD-L1
expressed on tumor cells and tumor-infiltrating immune cells,
preventing it from binding to PD-1 and B7.1 on the surface of T
cells. By inhibiting PD-L1, MPDL3280A may enable the activation of
T cells, restoring their ability to effectively detect and attack
tumor cells.
About Lung Cancer
According to the American Cancer Society, it is estimated that
more than 221,000 Americans will be diagnosed with lung cancer in
2015, and NSCLC accounts for 85 percent of all lung cancers. It is
estimated that approximately 60 percent of lung cancer diagnoses in
the United States are made when the disease is in the advanced
stages.
About Genentech in Lung Cancer
Lung cancer is a major area of focus and investment for
Genentech, and we are committed to developing new approaches,
medicines and tests that can help people with this deadly disease.
Our goal is to provide an effective treatment option for every
person diagnosed with lung cancer. We currently have two approved
medicines to treat certain kinds of lung cancer and more than 10
medicines being developed to target the most common genetic drivers
of lung cancer or to boost the immune system to combat the
disease.
About Genentech in Cancer Immunotherapy
For more than 30 years, Genentech has been developing medicines
with the goal to redefine treatment in oncology. Today, we’re
investing more than ever in our effort to bring innovative
treatment options that help a person’s own immune system fight
cancer. Our personalized cancer immunotherapy research and
development program comprises more than 20 investigational
candidates, seven of which are in clinical trials. All studies
include the evaluation of biomarkers to determine which people may
be appropriate candidates for our medicines.
About Genentech
Founded more than 35 years ago, Genentech is a leading
biotechnology company that discovers, develops, manufactures and
commercializes medicines to treat patients with serious or
life-threatening medical conditions. The company, a member of the
Roche Group, has headquarters in South San Francisco, California.
For additional information about the company, please visit
http://www.gene.com.
GenentechMedia Contact:Holli Dickson, 650-467-6800Advocacy
Contact:Jen Mills, 650-467-6722Investor Contacts:Eka Kortkhonjia,
650-467-5873Karl Mahler, 011 41 61 687 8503
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